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105310-47-2

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105310-47-2 Usage

Description

(E)-2-(Aminomethyl)-N,N-diethyl-1-phenylcyclopropanecarboxamide hydrochloride is a chemical compound characterized by a cyclopropane ring with an attached carboxamide group and an aminomethyl and diethyl groups. It is known for its potential as an analgesic or pain-relieving agent and is commonly used in the research and development of pharmaceuticals. The hydrochloride form of this compound enhances its solubility and stability, making it more suitable for laboratory work. Its unique structure and potential therapeutic applications make it a promising candidate in the field of medicinal chemistry and drug discovery.

Uses

Used in Pharmaceutical Research and Development:
(E)-2-(Aminomethyl)-N,N-diethyl-1-phenylcyclopropanecarboxamide hydrochloride is used as a research compound for the development of new pharmaceuticals, particularly for its potential as an analgesic agent. Its unique structure and properties make it a valuable tool in the discovery and optimization of novel pain-relieving drugs.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (E)-2-(Aminomethyl)-N,N-diethyl-1-phenylcyclopropanecarboxamide hydrochloride is used as a lead compound for the design and synthesis of new therapeutic agents. Its cyclopropane ring and functional groups provide a versatile scaffold for the exploration of structure-activity relationships and the development of more potent and selective analgesics.
Used in Drug Discovery:
(E)-2-(Aminomethyl)-N,N-diethyl-1-phenylcyclopropanecarboxamide hydrochloride is employed as a starting point in drug discovery efforts, where its chemical properties and potential therapeutic effects are further investigated and optimized. The hydrochloride form of the compound facilitates its use in various assays and screens, aiding in the identification of promising drug candidates for pain management and other therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 105310-47-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,3,1 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 105310-47:
(8*1)+(7*0)+(6*5)+(5*3)+(4*1)+(3*0)+(2*4)+(1*7)=72
72 % 10 = 2
So 105310-47-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H22N2O.ClH/c1-3-17(4-2)14(18)15(10-13(15)11-16)12-8-6-5-7-9-12;/h5-9,13H,3-4,10-11,16H2,1-2H3;1H/t13-,15-;/m0./s1

105310-47-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,2R)-2-(Aminomethyl)-N,N-diethyl-1-phenylcyclopropanecarboxamide hydrochloride

1.2 Other means of identification

Product number -
Other names (E)-2-(Aminomethyl)-N,N-diethyl-1-phenylcyclopropanecarboxamide hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:105310-47-2 SDS

105310-47-2Synthetic route

trans-2-aminomethyl-1-phenyl-N,N-diethylcyclopropanecarboxamide
105310-27-8

trans-2-aminomethyl-1-phenyl-N,N-diethylcyclopropanecarboxamide

Conditions
ConditionsYield
With hydrogenchloride In 1,4-dioxane at 20℃; for 1h;
trans-2-aminomethyl-1-phenyl-N,N-diethylcyclopropanecarboxamide
105310-27-8

trans-2-aminomethyl-1-phenyl-N,N-diethylcyclopropanecarboxamide

trans-2-aminomethyl-1-phenyl-N,N-diethylcyclopropanecarboxamide hydrochloride
105310-47-2

trans-2-aminomethyl-1-phenyl-N,N-diethylcyclopropanecarboxamide hydrochloride

Conditions
ConditionsYield
With hydrogenchloride In 1,4-dioxane at 20℃; for 1h;

105310-47-2Downstream Products

105310-47-2Relevant articles and documents

A new approach towards 1-phenyl and 1-benzyl substituted 2-(aminomethyl)cyclopropanecarboxamides as novel derivatives of the antidepressant Milnacipran

Vervisch, Karel,D'Hooghe, Matthias,Toernroos, Karl W.,De Kimpe, Norbert

experimental part, p. 3271 - 3279 (2009/10/24)

2-(2-Cyano-2-phenylethyl)aziridines were converted into novel trans-2-aminomethyl-1-phenylcyclopropanecarboxamides via regiospecific ring opening and 3-exo-tet cyclisation, thus providing the first convenient entry into the trans-isomer of Milnacipran as a useful template for further derivatisation. Furthermore, unprecedented 2-aminomethyl-1- benzylcyclopropanecarboxamides have been synthesized using two different routes starting from 2-(2-cyanoethyl)aziridines, both involving α-benzylation with respect to the nitrile group and aziridine to cyclopropane ring transformation. The Royal Society of Chemistry 2009.

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